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Spinal Muscular Atrophy A Timely Review
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Distal Hereditary Upper Limb Muscular Atrophy
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Hereditary Form of Parkinsonism-Dementia
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
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Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
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Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
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Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
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Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
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Progressive Pontobulbar Palsy With Deafness
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Epidemiology of Motor-Neuron Diseases
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Metabolic Disease and Stroke: MELAS
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Tourette's Syndrome:A Model Neuropsychiatric Disorder
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Niemann-Pick Type C Disease
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Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
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A 2-Year-Old Girl with Acute Encephalopathy After Febrile Systemic Illness
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Adult-Onset Coats Plus, A Case of Leukoencephalopathy with Calcifications, a Tumefactive Brain Lesion, and a Presumed Autoimmune Disease
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Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Alzheimers Disease
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Clinical Reasoning: A Teenager with Left Arm Weakness
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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